HGVS | Genome Assembly |
---|---|
NC_000003.12:g.169764618G>A , CM000665.2:g.169764618G>A | GRCh38 |
NC_000003.11:g.169482406G>A , CM000665.1:g.169482406G>A | GRCh37 |
NC_000003.10:g.170965100G>A | NCBI36 |
NG_016363.1:g.5443C>T , LRG_347:g.5443C>T |
HGVS | Amino-acid Change | |
---|---|---|
NR_001566.1:n.443C>T , LRG_347t1:n.443C>T |